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| | 2,6-Piperidinedione, 3-[4-(5-aminopentyl)-1,3-dihydro-1-oxo-2H-isoindol-2-yl]-, 2,2,2-trifluoroacetate (1:1) Basic information |
| Product Name: | 2,6-Piperidinedione, 3-[4-(5-aminopentyl)-1,3-dihydro-1-oxo-2H-isoindol-2-yl]-, 2,2,2-trifluoroacetate (1:1) | | Synonyms: | 2,6-Piperidinedione, 3-[4-(5-aminopentyl)-1,3-dihydro-1-oxo-2H-isoindol-2-yl]-, 2,2,2-trifluoroacetate (1:1);Lenalidomide-C5-NH2 (TFA) | | CAS: | 2550398-71-3 | | MF: | C20H24F3N3O5 | | MW: | 443.42 | | EINECS: | | | Product Categories: | | | Mol File: | 2550398-71-3.mol | ![2,6-Piperidinedione, 3-[4-(5-aminopentyl)-1,3-dihydro-1-oxo-2H-isoindol-2-yl]-, 2,2,2-trifluoroacetate (1:1) Structure](CAS/20211123/GIF/2550398-71-3.gif) |
| | 2,6-Piperidinedione, 3-[4-(5-aminopentyl)-1,3-dihydro-1-oxo-2H-isoindol-2-yl]-, 2,2,2-trifluoroacetate (1:1) Chemical Properties |
| form | Solid | | color | Light yellow to yellow |
| | 2,6-Piperidinedione, 3-[4-(5-aminopentyl)-1,3-dihydro-1-oxo-2H-isoindol-2-yl]-, 2,2,2-trifluoroacetate (1:1) Usage And Synthesis |
| Uses | Lenalidomide-C5-NH2 is the Lenalidomide-based Cereblon ligand used in the recruitment of CRBN protein. Lenalidomide-C5-NH2 can be connected to the ligand for protein by a linker to form PROTACs, such as MDM2 PROTAC degrader[1][2]. | | IC 50 | Cereblon | | References | [1] Zhou B, et al. Discovery of a Small-Molecule Degrader of Bromodomain and Extra-Terminal (BET) Proteins with Picomolar Cellular Potencies and Capable of Achieving Tumor Regression. J Med Chem. 2018;61(2):462-481. DOI:10.1021/acs.jmedchem.6b01816 [2] Li Y, Yang J, et al. Discovery of MD-224 as a First-in-Class, Highly Potent, and Efficacious Proteolysis Targeting Chimera Murine Double Minute 2 Degrader Capable of Achieving Complete and Durable Tumor Regression. J Med Chem. 2019;62(2):448-466. DOI:10.1021/acs.jmedchem.8b00909 |
| | 2,6-Piperidinedione, 3-[4-(5-aminopentyl)-1,3-dihydro-1-oxo-2H-isoindol-2-yl]-, 2,2,2-trifluoroacetate (1:1) Preparation Products And Raw materials |
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